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Biological impact of superparamagnetic iron oxide nanoparticles for magnetic particle imaging of head and neck cancer cells
BACKGROUND: As a tomographic imaging technology, magnetic particle imaging (MPI) allows high spatial resolution and sensitivity, and the possibility to create real-time images by determining the spatial distribution of magnetic particles. To ensure a prospective biosafe application of UL-D (Universi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4218924/ https://www.ncbi.nlm.nih.gov/pubmed/25378928 http://dx.doi.org/10.2147/IJN.S63873 |
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author | Lindemann, Antje Lüdtke-Buzug, Kerstin Fräderich, Bianca M Gräfe, Ksenija Pries, Ralph Wollenberg, Barbara |
author_facet | Lindemann, Antje Lüdtke-Buzug, Kerstin Fräderich, Bianca M Gräfe, Ksenija Pries, Ralph Wollenberg, Barbara |
author_sort | Lindemann, Antje |
collection | PubMed |
description | BACKGROUND: As a tomographic imaging technology, magnetic particle imaging (MPI) allows high spatial resolution and sensitivity, and the possibility to create real-time images by determining the spatial distribution of magnetic particles. To ensure a prospective biosafe application of UL-D (University of Luebeck-Dextran coated superparamagnetic nanoparticles), we evaluated the biocompatibility of superparamagnetic iron oxide nanoparticles (SPIONs), their impact on biological properties, and their cellular uptake using head and neck squamous cancer cells (HNSCCs). METHODS: SPIONs that met specific MPI requirements were synthesized as tracers. Labeling and uptake efficiency were analyzed by hematoxylin and eosin staining and magnetic particle spectrometry. Flow cytometry, 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assays, and real-time cell analyzer assays were used to investigate apoptosis, proliferation, and the cytokine response of SPION-labeled cells. The production of reactive oxygen species (ROS) was determined using a fluorescent dye. Experimental results were compared to the contrast agent Resovist(®), a standard agent used in MPI. RESULTS: UL-D nanoparticles and Resovist particles were taken up in vitro by HNSCCs via unspecific phagocytosis followed by cytosolic accumulation. To evaluate toxicity, flow cytometry analysis was performed; results showed that dose- and time-dependent administration of Resovist induced apoptosis whereas cell viability of UL-D-labeled cells was not altered. We observed decreased cell proliferation in response to increased SPION concentrations. An intracellular production of ROS could not be detected, suggesting that the particles did not cause oxidative stress. Tumor necrosis factor alpha (TNF-α) and interleukins IL-6, IL-8, and IL-1β were measured to distinguish inflammatory responses. Only the primary tumor cell line labeled with >0.5 mM Resovist showed a significant increase in IL-1β secretion. CONCLUSION: Our data suggest that UL-D SPIONs are a promising tracer material for use in innovative tumor cell analysis in MPI. |
format | Online Article Text |
id | pubmed-4218924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-42189242014-11-06 Biological impact of superparamagnetic iron oxide nanoparticles for magnetic particle imaging of head and neck cancer cells Lindemann, Antje Lüdtke-Buzug, Kerstin Fräderich, Bianca M Gräfe, Ksenija Pries, Ralph Wollenberg, Barbara Int J Nanomedicine Original Research BACKGROUND: As a tomographic imaging technology, magnetic particle imaging (MPI) allows high spatial resolution and sensitivity, and the possibility to create real-time images by determining the spatial distribution of magnetic particles. To ensure a prospective biosafe application of UL-D (University of Luebeck-Dextran coated superparamagnetic nanoparticles), we evaluated the biocompatibility of superparamagnetic iron oxide nanoparticles (SPIONs), their impact on biological properties, and their cellular uptake using head and neck squamous cancer cells (HNSCCs). METHODS: SPIONs that met specific MPI requirements were synthesized as tracers. Labeling and uptake efficiency were analyzed by hematoxylin and eosin staining and magnetic particle spectrometry. Flow cytometry, 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assays, and real-time cell analyzer assays were used to investigate apoptosis, proliferation, and the cytokine response of SPION-labeled cells. The production of reactive oxygen species (ROS) was determined using a fluorescent dye. Experimental results were compared to the contrast agent Resovist(®), a standard agent used in MPI. RESULTS: UL-D nanoparticles and Resovist particles were taken up in vitro by HNSCCs via unspecific phagocytosis followed by cytosolic accumulation. To evaluate toxicity, flow cytometry analysis was performed; results showed that dose- and time-dependent administration of Resovist induced apoptosis whereas cell viability of UL-D-labeled cells was not altered. We observed decreased cell proliferation in response to increased SPION concentrations. An intracellular production of ROS could not be detected, suggesting that the particles did not cause oxidative stress. Tumor necrosis factor alpha (TNF-α) and interleukins IL-6, IL-8, and IL-1β were measured to distinguish inflammatory responses. Only the primary tumor cell line labeled with >0.5 mM Resovist showed a significant increase in IL-1β secretion. CONCLUSION: Our data suggest that UL-D SPIONs are a promising tracer material for use in innovative tumor cell analysis in MPI. Dove Medical Press 2014-10-29 /pmc/articles/PMC4218924/ /pubmed/25378928 http://dx.doi.org/10.2147/IJN.S63873 Text en © 2014 Lindemann et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Lindemann, Antje Lüdtke-Buzug, Kerstin Fräderich, Bianca M Gräfe, Ksenija Pries, Ralph Wollenberg, Barbara Biological impact of superparamagnetic iron oxide nanoparticles for magnetic particle imaging of head and neck cancer cells |
title | Biological impact of superparamagnetic iron oxide nanoparticles for magnetic particle imaging of head and neck cancer cells |
title_full | Biological impact of superparamagnetic iron oxide nanoparticles for magnetic particle imaging of head and neck cancer cells |
title_fullStr | Biological impact of superparamagnetic iron oxide nanoparticles for magnetic particle imaging of head and neck cancer cells |
title_full_unstemmed | Biological impact of superparamagnetic iron oxide nanoparticles for magnetic particle imaging of head and neck cancer cells |
title_short | Biological impact of superparamagnetic iron oxide nanoparticles for magnetic particle imaging of head and neck cancer cells |
title_sort | biological impact of superparamagnetic iron oxide nanoparticles for magnetic particle imaging of head and neck cancer cells |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4218924/ https://www.ncbi.nlm.nih.gov/pubmed/25378928 http://dx.doi.org/10.2147/IJN.S63873 |
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